Sy M S, Lowy A, HayGlass K, Janeway C A, Gurish M, Greene M I, Benacerraf B
Proc Natl Acad Sci U S A. 1984 Jun;81(12):3846-50. doi: 10.1073/pnas.81.12.3846.
Prolonged treatment of mice, starting at birth, with rabbit anti-mouse mu-chain antibodies resulted in the elimination of immunoglobulin-bearing B cells in these animals. The ability of these animals to elicit antigen-specific delayed-type hypersensitivity or cytotoxic T-cell responses to azobenzenearsonate-coupled spleen cells was not impaired. The effect of anti-mu treatment on the restriction by immunoglobulin heavy-chain genes (Igh) of suppressor T cells was investigated. We found that first-order suppressor T-cell factor ( TsF1 ) obtained from anti-mu treated animals expresses an Igh restriction pattern distinct from that observed with TsF1 from normal untreated mice. Furthermore, TsF1 prepared from anti-mu treated animals did not express the major crossreactive idiotypic determinants normally present in TsF1 . The significance of these findings in relation to the role of immunoglobulin on the T-cell repertoire is discussed.
从出生开始用兔抗小鼠μ链抗体对小鼠进行长期治疗,导致这些动物体内携带免疫球蛋白的B细胞被清除。这些动物对偶氮苯砷酸盐偶联的脾细胞引发抗原特异性迟发型超敏反应或细胞毒性T细胞反应的能力并未受损。研究了抗μ治疗对抑制性T细胞免疫球蛋白重链基因(Igh)限制的影响。我们发现,从抗μ治疗的动物中获得的一级抑制性T细胞因子(TsF1)表达的Igh限制模式与从未经治疗的正常小鼠中获得的TsF1不同。此外,从抗μ治疗的动物中制备的TsF1不表达通常存在于TsF1中的主要交叉反应性独特型决定簇。讨论了这些发现与免疫球蛋白在T细胞库中的作用相关的意义。